JP2000063247A - カチオン性直接染料と増粘ポリマ―を含有するケラチン繊維の染色用組成物 - Google Patents

カチオン性直接染料と増粘ポリマ―を含有するケラチン繊維の染色用組成物

Info

Publication number: JP2000063247A
Authority: JP; Japan
Prior art keywords: chemical; group; composition; dyeing; alkyl
Prior art date: 1998-07-09
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

JP11196816A

Other languages

English (en)

Japanese (ja)

Inventor

Gerard Lang

ランジェラール

Jean Cotteret

コトレジャン

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

LOreal SA

Original Assignee

LOreal SA

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1998-07-09

Filing date

1999-07-09

Publication date

2000-02-29

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9528484&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=JP2000063247(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1999-07-09 Application filed by LOreal SA filed Critical LOreal SA

2000-02-29 Publication of JP2000063247A publication Critical patent/JP2000063247A/ja

Status Withdrawn legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 101
238000004043 dyeing Methods 0.000 title claims abstract description 86
239000000835 fiber Substances 0.000 title claims abstract description 29
239000000982 direct dye Substances 0.000 title claims abstract description 27
102000011782 Keratins Human genes 0.000 title claims abstract description 26
108010076876 Keratins Proteins 0.000 title claims abstract description 26
125000002091 cationic group Chemical group 0.000 title claims abstract description 26
229920000642 polymer Polymers 0.000 title claims abstract description 20
230000008719 thickening Effects 0.000 title claims abstract description 20
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 17
125000000217 alkyl group Chemical group 0.000 claims abstract description 16
229910052794 bromium Inorganic materials 0.000 claims abstract description 10
229910052801 chlorine Inorganic materials 0.000 claims abstract description 10
229920002907 Guar gum Polymers 0.000 claims abstract description 6
235000010417 guar gum Nutrition 0.000 claims abstract description 6
239000000665 guar gum Substances 0.000 claims abstract description 6
229960002154 guar gum Drugs 0.000 claims abstract description 6
241000196324 Embryophyta Species 0.000 claims abstract description 4
229920002472 Starch Polymers 0.000 claims abstract description 4
229920000615 alginic acid Polymers 0.000 claims abstract description 4
229920002678 cellulose Polymers 0.000 claims abstract description 4
235000010980 cellulose Nutrition 0.000 claims abstract description 4
239000001814 pectin Substances 0.000 claims abstract description 4
229920001277 pectin Polymers 0.000 claims abstract description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims abstract description 3
244000005700 microbiome Species 0.000 claims abstract 2
239000000126 substance Substances 0.000 claims description 92
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 18
230000001590 oxidative effect Effects 0.000 claims description 18
238000000034 method Methods 0.000 claims description 16
BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims description 12
239000007800 oxidant agent Substances 0.000 claims description 12
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 8
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
239000000460 chlorine Substances 0.000 claims description 8
229910052731 fluorine Inorganic materials 0.000 claims description 8
239000011737 fluorine Substances 0.000 claims description 8
239000011630 iodine Substances 0.000 claims description 8
229910052740 iodine Inorganic materials 0.000 claims description 8
230000003647 oxidation Effects 0.000 claims description 8
238000007254 oxidation reaction Methods 0.000 claims description 8
229910052717 sulfur Inorganic materials 0.000 claims description 8
125000005842 heteroatom Chemical group 0.000 claims description 6
229910052760 oxygen Inorganic materials 0.000 claims description 6
239000001301 oxygen Substances 0.000 claims description 6
239000002453 shampoo Substances 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 5
125000005843 halogen group Chemical group 0.000 claims description 5
229920002305 Schizophyllan Polymers 0.000 claims description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
238000009967 direct dyeing Methods 0.000 claims description 4
125000000623 heterocyclic group Chemical group 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
239000011593 sulfur Substances 0.000 claims description 4
125000004434 sulfur atom Chemical group 0.000 claims description 4
229920001285 xanthan gum Polymers 0.000 claims description 4
235000010493 xanthan gum Nutrition 0.000 claims description 4
239000000230 xanthan gum Substances 0.000 claims description 4
229940082509 xanthan gum Drugs 0.000 claims description 4
125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 3
229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
229920000569 Gum karaya Polymers 0.000 claims description 3
241000934878 Sterculia Species 0.000 claims description 3
235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 3
235000010418 carrageenan Nutrition 0.000 claims description 3
239000000679 carrageenan Substances 0.000 claims description 3
229920001525 carrageenan Polymers 0.000 claims description 3
229940113118 carrageenan Drugs 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
210000000416 exudates and transudate Anatomy 0.000 claims description 3
239000000451 gelidium spp. gum Substances 0.000 claims description 3
235000010494 karaya gum Nutrition 0.000 claims description 3
239000000231 karaya gum Substances 0.000 claims description 3
229940039371 karaya gum Drugs 0.000 claims description 3
239000003960 organic solvent Substances 0.000 claims description 3
UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 claims description 3
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
125000005263 alkylenediamine group Chemical group 0.000 claims description 2
150000001450 anions Chemical class 0.000 claims description 2
150000001555 benzenes Chemical group 0.000 claims description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 2
VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 2
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 2
229910052698 phosphorus Inorganic materials 0.000 claims description 2
229920001282 polysaccharide Polymers 0.000 claims description 2
239000005017 polysaccharide Substances 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims 2
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims 1
244000007835 Cyamopsis tetragonoloba Species 0.000 claims 1
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 claims 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
239000001785 acacia senegal l. willd gum Substances 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
239000001768 carboxy methyl cellulose Substances 0.000 claims 1
239000008112 carboxymethyl-cellulose Substances 0.000 claims 1
238000001035 drying Methods 0.000 claims 1
230000033444 hydroxylation Effects 0.000 claims 1
238000005805 hydroxylation reaction Methods 0.000 claims 1
125000004430 oxygen atom Chemical group O* 0.000 claims 1
239000012188 paraffin wax Substances 0.000 claims 1
238000010186 staining Methods 0.000 claims 1
229910021653 sulphate ion Inorganic materials 0.000 claims 1
238000005406 washing Methods 0.000 claims 1
244000215068 Acacia senegal Species 0.000 abstract description 3
229920000084 Gum arabic Polymers 0.000 abstract description 3
235000010489 acacia gum Nutrition 0.000 abstract description 3
239000000205 acacia gum Substances 0.000 abstract description 3
229910052739 hydrogen Inorganic materials 0.000 abstract description 3
235000010443 alginic acid Nutrition 0.000 abstract description 2
125000004181 carboxyalkyl group Chemical group 0.000 abstract description 2
239000001913 cellulose Substances 0.000 abstract description 2
239000007788 liquid Substances 0.000 abstract description 2
235000010987 pectin Nutrition 0.000 abstract description 2
235000019698 starch Nutrition 0.000 abstract description 2
FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 abstract 1
229940072056 alginate Drugs 0.000 abstract 1
239000008107 starch Substances 0.000 abstract 1
239000002562 thickening agent Substances 0.000 abstract 1
239000000975 dye Substances 0.000 description 14
150000001875 compounds Chemical class 0.000 description 9
239000002585 base Substances 0.000 description 8
244000303965 Cyamopsis psoralioides Species 0.000 description 6
229920000591 gum Polymers 0.000 description 6
241000282372 Panthera onca Species 0.000 description 5
238000004040 coloring Methods 0.000 description 5
-1 hydroxypropyl Chemical group 0.000 description 5
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
125000002768 hydroxyalkyl group Chemical group 0.000 description 3
108090000790 Enzymes Proteins 0.000 description 2
102000004190 Enzymes Human genes 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
229920000161 Locust bean gum Polymers 0.000 description 2
XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
229920001615 Tragacanth Polymers 0.000 description 2
239000002535 acidifier Substances 0.000 description 2
238000007792 addition Methods 0.000 description 2
239000000305 astragalus gummifer gum Substances 0.000 description 2
239000002610 basifying agent Substances 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
229940088598 enzyme Drugs 0.000 description 2
LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
239000002243 precursor Substances 0.000 description 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
FEBUJFMRSBAMES-UHFFFAOYSA-N 2-[(2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-phosphanyloxan-4-yl]oxy}-3,5-dihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-4-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl phosphinite Chemical compound OC1C(O)C(O)C(CO)OC1OCC1C(O)C(OC2C(C(OP)C(O)C(CO)O2)O)C(O)C(OC2C(C(CO)OC(P)C2O)O)O1 FEBUJFMRSBAMES-UHFFFAOYSA-N 0.000 description 1
NBOCQTNZUPTTEI-UHFFFAOYSA-N 4-[4-(hydrazinesulfonyl)phenoxy]benzenesulfonohydrazide Chemical compound C1=CC(S(=O)(=O)NN)=CC=C1OC1=CC=C(S(=O)(=O)NN)C=C1 NBOCQTNZUPTTEI-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
102100026189 Beta-galactosidase Human genes 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
240000008886 Ceratonia siliqua Species 0.000 description 1
235000013912 Ceratonia siliqua Nutrition 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
229920001503 Glucan Polymers 0.000 description 1
108010059881 Lactase Proteins 0.000 description 1
229930192627 Naphthoquinone Natural products 0.000 description 1
102000004316 Oxidoreductases Human genes 0.000 description 1
108090000854 Oxidoreductases Proteins 0.000 description 1
102000003992 Peroxidases Human genes 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
239000000420 anogeissus latifolia wall. gum Substances 0.000 description 1
239000001000 anthraquinone dye Substances 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
108010005774 beta-Galactosidase Proteins 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000000872 buffer Substances 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
229940106189 ceramide Drugs 0.000 description 1
150000001783 ceramides Chemical class 0.000 description 1
235000015165 citric acid Nutrition 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
239000006071 cream Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000000499 gel Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
229940015043 glyoxal Drugs 0.000 description 1
235000019314 gum ghatti Nutrition 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229920013821 hydroxy alkyl cellulose Polymers 0.000 description 1
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
229940116108 lactase Drugs 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
235000010420 locust bean gum Nutrition 0.000 description 1
239000000711 locust bean gum Substances 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
150000002791 naphthoquinones Chemical class 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
239000002304 perfume Substances 0.000 description 1
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JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
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239000003352 sequestering agent Substances 0.000 description 1
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150000003460 sulfonic acids Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
239000001003 triarylmethane dye Substances 0.000 description 1
AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
239000001018 xanthene dye Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B44/00—Azo dyes containing onium groups
- C09B44/10—Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system
- C09B44/14—1,2-Diazoles or hydrogenated 1,2-diazoles ; Pyrazolium; Indazolium
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4946—Imidazoles or their condensed derivatives, e.g. benzimidazoles
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides

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Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Cosmetics (AREA)

JP11196816A 1998-07-09 1999-07-09 カチオン性直接染料と増粘ポリマ―を含有するケラチン繊維の染色用組成物 Withdrawn JP2000063247A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR9808832A FR2780880B1 (fr)	1998-07-09	1998-07-09	Composition de teinture pour fibres keratiniques avec un colorant direct cationique et un polymere epaississant
FR9808832		1998-07-09

Publications (1)

Publication Number	Publication Date
JP2000063247A true JP2000063247A (ja)	2000-02-29

Family

ID=9528484

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP11196816A Withdrawn JP2000063247A (ja)	1998-07-09	1999-07-09	カチオン性直接染料と増粘ポリマ―を含有するケラチン繊維の染色用組成物

Country Status (16)

Country	Link
US (1)	US6613102B2 (de)
EP (1)	EP0970686B1 (de)
JP (1)	JP2000063247A (de)
KR (1)	KR100339287B1 (de)
CN (1)	CN1248435A (de)
AR (1)	AR019346A1 (de)
AT (1)	ATE324098T1 (de)
AU (1)	AU723986B2 (de)
BR (1)	BR9903125A (de)
CA (1)	CA2277355A1 (de)
DE (1)	DE69930994T2 (de)
ES (1)	ES2263261T3 (de)
FR (1)	FR2780880B1 (de)
HU (1)	HU221414B1 (de)
RU (1)	RU2179843C2 (de)
ZA (1)	ZA994229B (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2001335446A (ja) *	2000-04-18	2001-12-04	L'oreal Sa	１−（４−アミノフェニル）ピロリジンと特定の直接染料を含有するケラチン繊維の酸化染色用組成物
JP2001335445A (ja) *	2000-04-18	2001-12-04	L'oreal Sa	１−（４−アミノフェニル）ピロリジンと糖単位を有する増粘ポリマーを含有するケラチン繊維の酸化染色用組成物
JP2005532444A (ja) *	2002-07-05	2005-10-27	ロレアル	テトラアザペンタメチン化合物の直接染料としての使用および新規なテトラアザペンタメチン化合物
JP2008156354A (ja) *	2006-12-21	2008-07-10	L'oreal Sa	カチオン性界面活性剤、バイオヘテロポリサッカリド、両性界面活性剤、及び直接染料を含む直接染料組成物

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2780883B1 (fr) *	1998-07-09	2001-04-06	Oreal	Composition de teinture pour fibres keratiniques avec un colorant direct cationique et un polymere epaississant
KR20010034974A (ko) *	2000-05-10	2001-05-07	이병철	홈페이지 포탈 사이트 구축 및 관리 시스템
FR2912907B1 (fr) *	2007-02-23	2011-04-22	Oreal	Composition de coloration comprenant au moins un colorant azoique cationique a motif julolidine et au moins un polymere epaississant non cellulolique et procede de coloration
FR2971937B1 (fr) *	2011-02-25	2013-02-15	Oreal	Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un polymere epaississant non cellulosique, un agent alcalin, et un agent reducteur
FR2983730B1 (fr) *	2011-12-12	2014-01-31	Oreal	Composition cosmetique comprenant une combinaison de scleroglucane et de caroube, et utilisations.
FR2983729B1 (fr) *	2011-12-12	2014-01-31	Oreal	Composition cosmetique comprenant une combinaison de scleroglucane et d'agar, et utilisations.
FR3060319B1 (fr) *	2016-12-20	2019-05-24	L'oreal	Composition oxydante pour le traitement des fibres keratiniques comprenant une gomme de scleroglucane et un sequestrant phosphore
EP4013373A1 (de)	2019-08-14	2022-06-22	Kao Corporation	Färbezusammensetzung, verfahren, verwendung und teilesatz dafür

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GB1373081A (en) *	1970-11-06	1974-11-06	Unilever Ltd	Colourant compositions for keratinous fibres
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US3985499A (en)	1971-06-04	1976-10-12	L'oreal	Diazamerocyanines for dyeing keratinous fibers
US4153065A (en)	1972-06-19	1979-05-08	L'oreal	Azo derivatives of pyridine n-oxide for use in hair dye compositions
LU65539A1 (de)	1972-06-19	1973-12-21
US3915921A (en)	1974-07-02	1975-10-28	Goodrich Co B F	Unsaturated carboxylic acid-long chain alkyl ester copolymers and tri-polymers water thickening agents and emulsifiers
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US4509949A (en)	1983-06-13	1985-04-09	The B. F. Goodrich Company	Water thickening agents consisting of copolymers of crosslinked acrylic acids and esters
LU84875A1 (fr) *	1983-06-27	1985-03-29	Oreal	Compositions tinctoriales pour fibres keratiniques a base de colorants directs et de gomme de xanthane
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FR2586913B1 (fr)	1985-09-10	1990-08-03	Oreal	Procede pour former in situ une composition constituee de deux parties conditionnees separement et ensemble distributeur pour la mise en oeuvre de ce procede
FR2633940B3 (fr)	1988-07-05	1991-07-12	Sanofi Sa	Scleroglucane traite au glyoxal et son procede d'obtention
LU87338A1 (fr) *	1988-09-12	1990-04-06	Oreal	Utilisation de derives d'indole pour la teinture de matieres keratiniques,compositions tinctoriales,composes nouveaux et procede de teinture
GB9104878D0 (en)	1991-03-08	1991-04-24	Scott Bader Co	Thickeners for personal care products
TW311089B (de)	1993-07-05	1997-07-21	Ciba Sc Holding Ag
TW325998B (en)	1993-11-30	1998-02-01	Ciba Sc Holding Ag	Dyeing keratin-containing fibers
FR2722687A1 (fr) *	1994-07-22	1996-01-26	Oreal	Utilisation de gomme de guar dans des compositionsnon rincees pour la teinture des fibres keratiniques et procede de teinture
US5474578A (en)	1994-10-03	1995-12-12	Clairol, Inc.	Erasable hair dyeing process
EP1219683B1 (de)	1994-11-03	2004-03-24	Ciba SC Holding AG	Kationische Imidazolazofarbstoffe
DE19527978C2 (de) *	1995-07-31	1998-08-20	Kao Corp	Mittel zum Färben und Tönen von menschlichen Haaren und Verwendung von Hydroxy-C¶2¶_C¶4¶-alkyl-Guar-Gum in solchen Mitteln
DE59700027D1 (de) *	1996-04-20	1998-11-19	Goldwell Gmbh	Mittel zur Färbung und Tönung von menschlichen Haaren
GB9610378D0 (en)	1996-05-17	1996-07-24	Boots Co Plc	Hair colorant composition
FR2748931B1 (fr)	1996-05-23	1998-07-03	Oreal	Composition de teinture directe capillaire comprenant un polymere reticule a motifs acryliques et/ou acrylates et a motifs acrylamides
FR2750325B1 (fr)	1996-06-28	1998-07-31	Oreal	Utilisation en cosmetique d'un poly(acide 2-acrylamido 2- methylpropane sulfonique) reticule et neutralise a au moins 90 % et compositions topiques les contenant
FR2751533B1 (fr) *	1996-07-23	2003-08-15	Oreal	Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile non-ionique
FR2753094B1 (fr)	1996-09-06	1998-10-16	Oreal	Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile anionique
FR2753093B1 (fr)	1996-09-06	1998-10-16	Oreal	Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile anionique
FR2757388B1 (fr)	1996-12-23	1999-11-12	Oreal	Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition
FR2757384B1 (fr) *	1996-12-23	1999-01-15	Oreal	Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition
FR2757387B1 (fr) *	1996-12-23	1999-01-29	Oreal	Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition
FR2757385B1 (fr) *	1996-12-23	1999-01-29	Oreal	Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition
EP0920856B1 (de) *	1997-12-05	2004-01-28	L'oreal	Verfahren zur Direkt-Färbung von Keratin-Fasern in zwei Stufen mit Hilfe von Direct Basic Färbungsmitteln

1998
- 1998-07-09 FR FR9808832A patent/FR2780880B1/fr not_active Expired - Fee Related
1999
- 1999-06-22 AT AT99401548T patent/ATE324098T1/de not_active IP Right Cessation
- 1999-06-22 DE DE69930994T patent/DE69930994T2/de not_active Revoked
- 1999-06-22 EP EP99401548A patent/EP0970686B1/de not_active Revoked
- 1999-06-22 ES ES99401548T patent/ES2263261T3/es not_active Expired - Lifetime
- 1999-06-28 ZA ZA9904229A patent/ZA994229B/xx unknown
- 1999-06-28 AU AU36808/99A patent/AU723986B2/en not_active Ceased
- 1999-07-02 KR KR1019990026616A patent/KR100339287B1/ko not_active IP Right Cessation
- 1999-07-07 BR BR9903125-6A patent/BR9903125A/pt not_active IP Right Cessation
- 1999-07-08 US US09/349,436 patent/US6613102B2/en not_active Expired - Fee Related
- 1999-07-08 CN CN99119516A patent/CN1248435A/zh active Pending
- 1999-07-08 RU RU99115091/14A patent/RU2179843C2/ru not_active IP Right Cessation
- 1999-07-08 HU HU9902332A patent/HU221414B1/hu not_active IP Right Cessation
- 1999-07-08 AR ARP990103320A patent/AR019346A1/es not_active Application Discontinuation
- 1999-07-08 CA CA002277355A patent/CA2277355A1/fr not_active Abandoned
- 1999-07-09 JP JP11196816A patent/JP2000063247A/ja not_active Withdrawn

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2001335446A (ja) *	2000-04-18	2001-12-04	L'oreal Sa	１−（４−アミノフェニル）ピロリジンと特定の直接染料を含有するケラチン繊維の酸化染色用組成物
JP2001335445A (ja) *	2000-04-18	2001-12-04	L'oreal Sa	１−（４−アミノフェニル）ピロリジンと糖単位を有する増粘ポリマーを含有するケラチン繊維の酸化染色用組成物
JP2005532444A (ja) *	2002-07-05	2005-10-27	ロレアル	テトラアザペンタメチン化合物の直接染料としての使用および新規なテトラアザペンタメチン化合物
JP2008156354A (ja) *	2006-12-21	2008-07-10	L'oreal Sa	カチオン性界面活性剤、バイオヘテロポリサッカリド、両性界面活性剤、及び直接染料を含む直接染料組成物

Also Published As

Publication number	Publication date
EP0970686A1 (de)	2000-01-12
DE69930994T2 (de)	2007-01-04
KR20000011443A (ko)	2000-02-25
ATE324098T1 (de)	2006-05-15
CA2277355A1 (fr)	2000-01-09
KR100339287B1 (ko)	2002-06-03
DE69930994D1 (de)	2006-06-01
RU2179843C2 (ru)	2002-02-27
AU723986B2 (en)	2000-09-07
HUP9902332A2 (hu)	2000-03-28
US6613102B2 (en)	2003-09-02
AU3680899A (en)	2000-02-03
FR2780880B1 (fr)	2001-08-10
AR019346A1 (es)	2002-02-13
ZA994229B (en)	2000-01-12
HU9902332D0 (en)	1999-09-28
EP0970686B1 (de)	2006-04-26
US20020010968A1 (en)	2002-01-31
FR2780880A1 (fr)	2000-01-14
HUP9902332A3 (en)	2000-11-28
US20030005525A9 (en)	2003-01-09
ES2263261T3 (es)	2006-12-01
BR9903125A (pt)	2000-05-30
CN1248435A (zh)	2000-03-29
HU221414B1 (en)	2002-09-28

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Date	Code	Title	Description
2005-01-25	A02	Decision of refusal	Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20050125
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2005-07-27	A911	Transfer to examiner for re-examination before appeal (zenchi)	Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20050726
2005-10-11	A912	Re-examination (zenchi) completed and case transferred to appeal board	Free format text: JAPANESE INTERMEDIATE CODE: A912 Effective date: 20051007
2006-04-11	A761	Written withdrawal of application	Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20060410

Publication	Publication Date	Title
JP3348066B2 (ja)	2002-11-20	新規アゾ化合物、染色におけるその使用、該化合物を含む組成物及び染色方法
JP3609428B2 (ja)	2005-01-12	ケラチン繊維を染色するための組成物、および該組成物を用いた染色方法
JP2000063246A (ja)	2000-02-29	カチオン性直接染料と増粘ポリマ―を含有するケラチン繊維の染色用組成物
CA2138479C (fr)	2000-07-25	Composition de teinture d'oxydation des fibres keratiniques comprenant une paraphenylenediamine a fonction amine primaire, secondaire ou tertiaire, une metaphenylenediamine et un para-aminophenol ou un meta-aminophenol, et procede de teinture utilisant une telle composition
JP2008044959A (ja)	2008-02-28	カチオン性直接着色剤と第４級アンモニウム塩を含有するケラチン繊維の染色用組成物
FR2735685A1 (fr)	1996-12-27	Compositions pour la teinture des fibres keratiniques comprenant un ortho-diamino pyrazole et un sel de manganese procede de teinture mettant en oeuvre ces compositions
MXPA99006367A (en)	2000-12-06	Dyeing composition for keratinic fibers with a cationic direct coloring and a polymer espesa
JP2000063247A (ja)	2000-02-29	カチオン性直接染料と増粘ポリマ―を含有するケラチン繊維の染色用組成物
JP2710589B2 (ja)	1998-02-10	ケラチン繊維の染色セット、染色方法、染色ユニットおよび染色組成物
WO1997002008A1 (fr)	1997-01-23	Procede de teinture d'oxydation en deux temps des fibres keratiniques avec un sel de manganese et un colorant d'oxydation et kit de teinture
US5873910A (en)	1999-02-23	Process for the two-stage oxidation dyeing of keratin fibers with a manganese complex or salt and a 4-substituted 1-naphthol, and dyeing kit
CA2137993C (fr)	1999-09-07	Composition de teinture d'oxydation des fibres keratiniques comprenant un 3-fluoroparaaminophenol, un metaaminophenol et/ou une metaphenylene diamine et procede de teinture utilisant une telle composition
EP0728463B1 (de)	1999-07-21	Oxidationshaarfärbezusammensetzung, enthaltend mindestens zwei Oxidationsbasen und einen Indolkuppler und Färbeverfahren
JP2880113B2 (ja)	1999-04-05	ケラチン繊維の酸化染色用組成物およびこの組成物を用いた染色方法
CZ237299A3 (cs)	2000-01-12	Prostředek pro barvení keratinových vláken obsahující kationické přímé barvivo a zahušťovací polymer
EP1559410A1 (de)	2005-08-03	Keratinfaserfärbemittel enthaltend eine Alkohol-Oxydase und ein Polymer auf Basis von Zucker
CZ237099A3 (cs)	2000-01-12	Prostředek pro barvení keratinových vláken obsahující kationické přímé barvivo a ' zahušťovací polymer
MXPA99006326A (en)	2000-08-01	Dyeing composition for keratinic fibers with a cationic direct coloring and a polymer espesa
BE894633A (fr)	1983-04-07	Composition tinctoriale pour fibres keratiniques a base de nitroanilines, nouvelles nitroanilines et leur procede de preparation

JP2000063247A - カチオン性直接染料と増粘ポリマ―を含有するケラチン繊維の染色用組成物 - Google Patents

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